MICROWAVE SYNTHESIS OF 3- AND 4-SUBSTITUTED-5-((3-PHENYLPROPYL)THIO)-4H-1,2,4-TRIAZOLES

Yıl 2021, Cilt: 45 Sayı: 3, 457 - 466, 27.09.2021

Andrey Safonov Alina Nevmyvaka Oleksandr Panasenko Yevgenii Knysh

https://doi.org/10.33483/jfpau.902274

Cited By: 3

Öz

Objective: The purpose of this work was to synthesize 3- and 4-substituted-5-((3-phenylpropyl)thio) 4H-1,2,4-triazoles by the Milestone Flexi Wave microwave synthesis system and choose the best method of synthesis.

Material and Method: The initial compounds 4-amino-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole-3-thiol (1) and 5-(2-bromophenyl)-4-phenyl-4H-1,2,4-triazole-3-thiol (3) were synthesized at the Department of Natural Sciences for Foreign Students and Toxicological Chemistry of the Zaporizhzhya State Medical University (Ukraine). Milestone Flexi Wave microwave synthesis system was used to synthesize 3- and 4-substituted-5-((3-phenylpropyl)thio)-4H-1,2,4-triazoles. The elemental analysis of synthesized compounds was established by the universal analyzer Elementar Vario L cube (CHNS). The 1H spectra (at 400 MHz) were recorded in DMSO-d6 on a Varian MR-400 spectrometer and analyzed with ADVASP™ Analyzer program. The gas chromatograph Agilent 7890B with a 5977B mass spectrometry detector (US) was used to define the completeness of the reactions and the individuality of the resulting compounds.

Result and Discussion: The reaction was carried out in i-propanol medium and an equivalent amount of sodium hydroxide. (3-Bromopropyl)benzene was added to starting substances 1 and 3. To study the completeness of the reaction, different reaction times were used. Conditions such as temperature, microwave radiation, pressure were unchanged. The temperature of the reaction mixture was kept at 1650C, pressure 12.2 bar, MW ≈ 540 W. The reaction time was set at 15 minutes, 30 minutes, and 45 minutes. The most effective reaction time for obtaining 3-(thiophen-2-ylmethyl)-4-amino-5-((3-phenylpropyl)thio)-4H-1,2,4-triazole (2) is 45 minutes. The most energy efficient reaction time for 3-(2-bromophenyl)-4-phenyl-5-((3-phenylpropyl)thio)-4H-1,2,4-triazole (4) is 30 minutes heating. The signals of 1H NMR for compounds 2 and 4 are consented with the proposed structure. The elemental analysis (CHNS) was accomplished for synthesized compounds to confirm their basic chemical structures and revealed acceptable agreement with the calculated percentages

Anahtar Kelimeler

1,2,4-triazole, synthesis, 1HNMR, gas chromatography, heterocyclic compounds

Teşekkür

We're grateful to the Zaporizhzhya State Medical University for providing some facilities in carrying out the research.

3- VE 4-SÜBSTİTÜE-5-((3-FENİLPROPİL)TİYO)-4H-1,2,4-TRİAZOLLERİN MİKRODALGA SENTEZİ

Öz

Amaç: Bu çalışmanın amacı, Milestone Flexi Wave mikrodalga sentez sistemi ile 3- ve 4-sübstitüe-5-((3-fenilpropil)tiyo)-4H-1,2,4-triazolleri sentezlemek ve sentez için en iyi yöntemi belirlemektir.

Gereç ve Yöntem: Başlangıç bileşikleri olan 4-amino-5-(tiyofen-2-il-metil)-4H-1,2,4-triazol-3-tiyol (1) ve 5-(2-bromofenil)-4-fenil-4H-1,2,4-triazol-3-tiyol (3), Zaporizhzhya Devlet Tıp Üniversitesi (Ukrayna) Yabancı Öğrenciler için Doğa Bilimleri ve Toksikolojik Kimya Bölümü’nde sentezlendi. 3- ve 4-Sübstitüe-5-((3-fenilpropil)tiyo)-4H-1,2,4-triazolleri sentezlemek için Milestone Flexi Wave mikrodalga sentez sistemi kullanıldı. Sentezlenen bileşiklerin elementel analizi, Elementar Vario L cube (CHNS) evrensel analiz cihazı ile gerçekleştirildi. 1H-NMR spektrumları (400 MHz), DMSO-d6 içerisinde Varian MR-400 spektrometresi ile çekildi ve ADVASP™ Analiz programı ile analiz edildi. Reaksiyonların tamamlanıp tamamlanmadığı ve elde edilen bileşiklerin tayini, 5977B kütle spektrometre detektörü içeren Agilent 7890B gaz kromatografısi ile gerçekleştirildi.

Sonuç ve Tartışma: Reaksiyon, i-propanol içerisinde ve eşdeğer miktarda sodyum hidroksit varlığında gerçekleştirildi. Başlangıç maddeleri 1 ve 3'e (3-bromopropil)benzen eklendi. Reaksiyonun tam olarak sonlanmasının takibi için farklı reaksiyon süreleri kullanıldı. Sıcaklık, mikrodalga radyasyonu, basınç gibi koşullar değiştirilmedi. Reaksiyon ortamının sıcaklığı 1650C'de, basınç 12.2 bar'da, MW ≈ 540 W'da tutuldu. Reaksiyon süresi 15 dakika, 30 dakika ve 45 dakikaya ayarlandı. 3-(Tiyofen-2-il-metil)-4-amino-5-((3-fenilpropil)tiyo)-4H-1,2,4-triazol (2) elde etmek için en uygun reaksiyon süresi 45 dakikadır. 3-(2-Bromofenil)-4-fenil-5-((3-fenilpropil)tiyo)-4H-1,2,4-triazol (4) için en uygun reaksiyon süresi 30 dakika ısıtma olarak bulundu. Bileşik 2 ve 4 için 1H NMR sinyalleri, önerilen yapı ile uyumludur. Sentezlenen bileşiklerin kimyasal yapılarını doğrulamak için elementel analiz (CHNS) yapıldı ve hesaplanan yüzdeler kabul edilebilir aralıkta bulundu.

Anahtar Kelimeler

Gaz kromatografisi, heterosiklik bileşikler, 1H NMR, sentez, 1.2.4-triazol

Kaynakça

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